chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	12606344	12606345	G	A	28	GENIC	homozygous	115570254
7	12606416	12606417	T	C	22	GENIC	homozygous	115570255
7	12606947	12606948	A	T	30	GENIC	homozygous	115570256
7	12606957	12606958	G	A	31	GENIC	homozygous	115570257
7	12607017	12607018	T	G	16	GENIC	homozygous	115570258
7	12607024	12607025	C	T	17	GENIC	possibly homozygous	115570259
7	12607316	12607317	A	G	19	GENIC	homozygous	115570260
7	12607356	12607357	G	A	34	GENIC	homozygous	115570261
7	12607357	12607358	C	A	34	GENIC	homozygous	115570262
7	12607420	12607421	C	A	41	GENIC	homozygous	115570263
7	12608061	12608062	G	C	41	GENIC	homozygous	115570265
7	12608442	12608443	G	A	33	GENIC	homozygous	115570266
7	12609374	12609375	G	T	22	GENIC	homozygous	115570267
7	12609394	12609395	C	T	24	GENIC	homozygous	115570268
7	12609713	12609714	T	C	40	GENIC	homozygous	115570269